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Arif B Ekici

Showing results (1-10 of 299) with videos related to

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Scientific Data|September 12, 2018
Single-cell RNA sequencing of adult mouse testesSoeren Lukassen, Elisabeth Bosch, Arif B Ekici, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 14, 2011
Evaluation of conserved and ultra-conserved non-genic sequences in chromosome 15q15-linked periodic catatoniaDenny Schanze, Arif B Ekici, Bruno Pfuhlmann, et al.
Herz|October 31, 2006
[Gene polymorphisms leading to calcified and stenotic aortic valves]Thomas Anger, Arif B Ekici, Werner G Daniel, et al.
Plos One|May 19, 2015
Novel loci for non-syndromic coarctation of the aorta in sporadic and familial casesJulia Moosmann, Steffen Uebe, Sven Dittrich, et al.
BMC Bioinformatics|September 23, 2010
GPFrontend and GPGraphics: graphical analysis tools for genetic association studiesSteffen Uebe, Francesca Pasutto, Mandy Krumbiegel, et al.
Scientific Reports|November 5, 2020
Loss of PHF6 leads to aberrant development of human neuron-like cellsAnna Fliedner, Anne Gregor, Fulvia Ferrazzi, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
A new quantitative PCR multiplex assay for rapid analysis of chromosome 17p11.2-12 duplications and deletions leading to HMSN/HNPPChristian T Thiel, Cornelia Kraus, Anita Rauch, et al.
European Journal of Medical Genetics|September 2, 2008
6.7 Mb interstitial duplication in chromosome band 11q24.2q25 associated with infertility, minor dysmorphic features and normal psychomotor developmentIna Göhring, Hans-Martin Blümlein, Juliane Hoyer, et al.
American Journal of Medical Genetics. Part A|November 20, 2018
Microphthalmia is not a mandatory finding in X-linked recessive syndromic microphthalmia caused by the recurrent BCOR variant p.Pro85LeuCornelia Kraus, Steffen Uebe, Christian T Thiel, et al.
American Journal of Medical Genetics. Part A|May 26, 2017
Haploinsufficiency of NR4A2 is associated with a neurodevelopmental phenotype with prominent language impairmentMiriam S Reuter, Mandy Krumbiegel, Gregor Schlüter, et al.
Pageof 30

Showing results (1-10 of 299) with videos related to

Sort By:
Pageof 30
Scientific Data|September 12, 2018
Single-cell RNA sequencing of adult mouse testesSoeren Lukassen, Elisabeth Bosch, Arif B Ekici, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 14, 2011
Evaluation of conserved and ultra-conserved non-genic sequences in chromosome 15q15-linked periodic catatoniaDenny Schanze, Arif B Ekici, Bruno Pfuhlmann, et al.
Herz|October 31, 2006
[Gene polymorphisms leading to calcified and stenotic aortic valves]Thomas Anger, Arif B Ekici, Werner G Daniel, et al.
Plos One|May 19, 2015
Novel loci for non-syndromic coarctation of the aorta in sporadic and familial casesJulia Moosmann, Steffen Uebe, Sven Dittrich, et al.
BMC Bioinformatics|September 23, 2010
GPFrontend and GPGraphics: graphical analysis tools for genetic association studiesSteffen Uebe, Francesca Pasutto, Mandy Krumbiegel, et al.
Scientific Reports|November 5, 2020
Loss of PHF6 leads to aberrant development of human neuron-like cellsAnna Fliedner, Anne Gregor, Fulvia Ferrazzi, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
A new quantitative PCR multiplex assay for rapid analysis of chromosome 17p11.2-12 duplications and deletions leading to HMSN/HNPPChristian T Thiel, Cornelia Kraus, Anita Rauch, et al.
European Journal of Medical Genetics|September 2, 2008
6.7 Mb interstitial duplication in chromosome band 11q24.2q25 associated with infertility, minor dysmorphic features and normal psychomotor developmentIna Göhring, Hans-Martin Blümlein, Juliane Hoyer, et al.
American Journal of Medical Genetics. Part A|November 20, 2018
Microphthalmia is not a mandatory finding in X-linked recessive syndromic microphthalmia caused by the recurrent BCOR variant p.Pro85LeuCornelia Kraus, Steffen Uebe, Christian T Thiel, et al.
American Journal of Medical Genetics. Part A|May 26, 2017
Haploinsufficiency of NR4A2 is associated with a neurodevelopmental phenotype with prominent language impairmentMiriam S Reuter, Mandy Krumbiegel, Gregor Schlüter, et al.
Pageof 30